US4662935AExpiredUtility
Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers
Est. expiryJan 14, 2000(expired)· nominal 20-yr term from priority
C07C 205/43C07C 205/38C07D 303/24C07C 205/59C07C 205/12
32
PatentIndex Score
0
Cited by
5
References
17
Claims
Abstract
Compounds of the formula ##STR1## wherein X is a hydrogen atom, a halogen atom, a trihalomethyl group, an alkyl group, or a cyano group, Y is a hydrogen atom, a halogen atom, or a trihalomethyl group, and Z is a substituted alkoxy group, and compositions containing these compounds exhibit herbicidal activity.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A herbicidal composition which comprises a compound of the formula ##STR9## wherein X is a hydrogen atom, a halogen atom, a trifluoromethyl group, or a (C 1 -C 4 ) alkyl group, Y is a hydrogen atom, a halogen atom, or a trifluoromethyl group, and Z is an unsubstituted amino group, an amino group having one or both hydrogen atoms replaced by one or two unsubstituted or halo-, hydroxy- or alkoxy-substituted alkyl groups having a total of up to 6 carbon atoms and an agronomically-acceptable carrier.
2. A composition according to claim 1 which also comprises a surfactant.
3. A method of controlling weeds which comprises applying to the surface of the growth medium prior to the emergence of the weeds from the growth medium a compound according to claim 1 in an amount sufficient to control the growth of the weeds.
4. The method of claim 3 wherein the compound is applied at a rate of about 0.1 to about 12 pounds per acre.
5. A method of controlling weeds which comprises applying to weed seedlings a compound of the formula ##STR10## wherein X is a hydrogen atom, a halogen atom, a trifluoromethyl group, or a (C 1 -C 4 ) alkyl group, Y is a hydrogen atom, a halogen atom, or a trifluoromethyl group, and Z is an unsubstituted amino group, an amino group having one or both hydrogen atoms replaced by one or two unsubstituted or halo-, hydroxy- or alkoxy-substituted alkyl groups having a total of up to 6 carbon atoms and an agronomically-acceptable carrier.
6. The method of claim 5 wherein the compound is applied at a rate of about 0.1 to about 12 pounds per acre.
7. The method of claim 4 wherein X is a chlorine atom and Z is an unsubstituted amino group.
8. The method of claim 4 wherein Z is an alkylamino group.
9. The method of claim 8 wherein X is a chlorine atom and Z is an ethylamino group.
10. The method according to claim 4 wherein Z is a dialkylamino group.
11. The method of claim 10 wherein X is a chlorine atom and Z is a dimethylamino group.
12. The method of claim 10 wherein X is a chlorine atom and Z is diethylamino group.
13. The method according to claim 10 wherein X is a chlorine atom and Z is a dipropylamino group.
14. The method according to claim 4 wherein Z is a halo-, hydro-, or alkoxy-substituted alkylamino group.
15. The method according to claim 4 wherein X is a chlorine atom and Z is a hydroxyethylamino group.
16. The method according to claim 12 wherein X is a chlorine atom and Z is a hydroxymethylethylamino group.
17. The method according to claim 12 wherein X is a chlorine atom and Z is a hydroxyethylethylamino group.Cited by (0)
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